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Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD

[Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester...

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Autor principal: Turhanen, Petri A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044877/
https://www.ncbi.nlm.nih.gov/pubmed/30023676
http://dx.doi.org/10.1021/acsomega.7b00531
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author Turhanen, Petri A.
author_facet Turhanen, Petri A.
author_sort Turhanen, Petri A.
collection PubMed
description [Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester of ATP (ApppI). Very recently, ApppI has been found to possess novel function(s); now it will also be possible to examine the effects of ApppD more precisely because it can be synthesized in reasonable amounts. 1-Adenosin-5′-yl 3-(3-methylbut-2-enyl) diphosphoric acid diester (AppD; a adenosine diphosphate analogue) was also isolated from the synthesis mixture. Both ApppD and AppD were characterized by (1)H, (13)C, (31)P NMR and mass spectrometry methods.
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spelling pubmed-60448772018-07-16 Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD Turhanen, Petri A. ACS Omega [Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester of ATP (ApppI). Very recently, ApppI has been found to possess novel function(s); now it will also be possible to examine the effects of ApppD more precisely because it can be synthesized in reasonable amounts. 1-Adenosin-5′-yl 3-(3-methylbut-2-enyl) diphosphoric acid diester (AppD; a adenosine diphosphate analogue) was also isolated from the synthesis mixture. Both ApppD and AppD were characterized by (1)H, (13)C, (31)P NMR and mass spectrometry methods. American Chemical Society 2017-06-21 /pmc/articles/PMC6044877/ /pubmed/30023676 http://dx.doi.org/10.1021/acsomega.7b00531 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Turhanen, Petri A.
Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title_full Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title_fullStr Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title_full_unstemmed Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title_short Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
title_sort synthesis of a biologically important adenosine triphosphate analogue, apppd
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044877/
https://www.ncbi.nlm.nih.gov/pubmed/30023676
http://dx.doi.org/10.1021/acsomega.7b00531
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